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3-Chloroperoxybenzoic Acid

    • Product Name 3-Chloroperoxybenzoic Acid
    • Alias mCPBA
    • Einecs 226-135-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    Specifications

    HS Code

    785524

    Chemicalname 3-Chloroperoxybenzoic Acid
    Molecularformula C7H5ClO3
    Molarmass 172.57 g/mol
    Casnumber 937-14-4
    Appearance White to off-white crystalline powder
    Meltingpoint 77-82 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Boilingpoint Decomposes before boiling
    Density 1.68 g/cm³
    Storagetemperature Store at 2-8 °C

    As an accredited 3-Chloroperoxybenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Chloroperoxybenzoic Acid, 100g, is packaged in a sealed amber glass bottle with hazard labeling and a secure, chemical-resistant cap.
    Shipping 3-Chloroperoxybenzoic acid (m-CPBA) is shipped as a hazardous material, typically in tightly sealed, corrosion-resistant containers. It requires cool, dry conditions, away from combustible and reducing materials. Transport is subject to international and local regulations due to its strong oxidizing properties and potential health hazards. Handle with appropriate safety precautions.
    Storage 3-Chloroperoxybenzoic acid (mCPBA) should be stored in a cool, dry, and well-ventilated area away from heat, light, and combustible materials. Keep it tightly closed in its original container, preferably refrigerated (2–8°C). Due to its sensitivity to shock and contamination, handle with care and avoid friction or impact. Store separately from reducing agents, acids, and bases.
    Application of 3-Chloroperoxybenzoic Acid

    Purity 77%: 3-Chloroperoxybenzoic Acid with a purity of 77% is used in epoxidation reactions, where it ensures high conversion rates and minimal by-product formation.

    Active Oxygen Content: 3-Chloroperoxybenzoic Acid with an active oxygen content of 6.5% is used in oxidative cleavage processes, where it delivers enhanced oxidation efficiency.

    Melting Point 106°C: 3-Chloroperoxybenzoic Acid of melting point 106°C is used in laboratory organic synthesis, where its defined phase transition facilitates precise temperature-controlled reactions.

    Particle Size <200 µm: 3-Chloroperoxybenzoic Acid with particle size under 200 µm is used in fine chemical manufacturing, where the small granule size improves reactivity and dispersion kinetics.

    Moisture Content <1%: 3-Chloroperoxybenzoic Acid with less than 1% moisture content is used in pharmaceutical intermediate synthesis, where low water concentration preserves peracid stability.

    Stability Temperature up to 40°C: 3-Chloroperoxybenzoic Acid stable up to 40°C is used in scaled production environments, where its thermal endurance maintains oxidizing power during storage.

    Assay ≥75%: 3-Chloroperoxybenzoic Acid with an assay value of at least 75% is used in selective oxidation of sulfides, where it ensures accurate stoichiometric control and predictable yields.

    Free Acid Content <1%: 3-Chloroperoxybenzoic Acid with free acid content below 1% is used in fluorination reactions, where low acidity prevents unwanted side reactions and product degradation.

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    Certification & Compliance
    More Introduction

    Discovering the Benefits of 3-Chloroperoxybenzoic Acid in Modern Chemistry

    3-Chloroperoxybenzoic Acid, often referred to as mCPBA in labs, has quietly shaped the way chemical transformations are carried out every day. For chemists, both academic and industrial, it opens doors that older oxidizing agents sometimes leave firmly shut. Talking to fellow researchers, the first thing that comes to mind about mCPBA is reliability. Across hundreds of experiments and pilot plant runs, this crystalline white solid brings results with clarity—freeing us from surprises common with less stable reagents.

    I’ve watched teams in organic synthesis lean toward 3-Chloroperoxybenzoic Acid for one main reason: control. In oxidative reactions, especially when dealing with sensitive molecules, mCPBA pushes reactions in predictable directions. In my own career synthesizing pharmaceuticals, it has turned difficult epoxidations into walk-in-the-park procedures. We see this frequently in the lab, especially during the conversion of alkenes to epoxides, or transforming sulfides into sulfoxides and sulfones, each step demanding care to avoid over-oxidation or unwanted byproducts. With mCPBA, the margin for error feels wider and results come closer to theoretical yield than with older peroxides or peracids.

    Model and Specifications Matter in the Real World

    Not all batches—or brands—of 3-Chloroperoxybenzoic Acid act the same. My earliest experience involved a generic laboratory-grade sample with an active content just over 70%. The implications went beyond paperwork: impurities dragged down selectivity, and reactions produced more side-products than anyone preferred. Commercially available mCPBA commonly ranges from 70% to 77% purity, balanced with m-chlorobenzoic acid and minor stabilizers to improve shelf life and handling safety. In industry, knowing the precise active oxygen content of each lot is crucial. Quality control teams always weigh and titrate each fresh sample before scaling up; working blind with oxidizers feels like walking a tightrope.

    Stability is a huge concern. Unlike some peracids that break down unpredictably, 3-Chloroperoxybenzoic Acid, when stored cool and dry, resists decomposition over months—sometimes years. Well-sealed containers tucked away from light and heat keep it ready for action when projects call. I’ve learned to keep fresh, desiccated samples for high-sensitivity applications; old or misstored bottles bring trouble, from reduced potency to unpredictably vigorous reactions. Laboratories often set reminders to check the active content every few months, a routine that saves cost and time in the long run.

    Usage Is Shaped by Real Experience

    The classroom teaches oxidizing power; the lab teaches how it plays out in real reactions. mCPBA regularly serves as a key player for epoxidation of alkenes, Baeyer–Villiger oxidations of ketones, and oxidative cleavage in multi-step syntheses. Selectivity really stands out, especially with substrates prone to rearrangement or decomposition. Peers working on natural product total synthesis or active pharmaceutical ingredients swear by its ability to perform challenging oxidations without wrecking sensitive groups elsewhere on the molecule. In my own work, the one-pot transformations achieved with mCPBA outpaced those with hydrogen peroxide, running smoother and offering fewer headaches during purification.

    I remember early reactions where a mix of oxidizers muddied the waters—too many incompletely oxidized byproducts, degradation of starting material, and extended chromatography that cost both time and solvents. Once mCPBA became standard, columns slimmed down, product isolation improved, and the number of purification steps dropped. Oxidations, often seen as delicate, unpredictable stages in synthesis, settled into routine procedures handled by junior chemists with confidence. The consistent, moderate reactivity paired with manageable safety risks put it front and center for both bench and pilot-scale chemistry.

    Industries outside academia have cottoned on, too. From specialty polymers to agrochemicals, production teams appreciate the fact that a well-characterized oxidizer means fewer hiccups. Reaction exotherms stay within manageable limits, and side-products become traceable rather than unpredictable. Plant operators see smoother workflows, reduction of hazard scenarios, and a more transparent process from feedstock to final product. Having visited a handful of plants myself, safety briefings rarely feature mCPBA as a primary concern, as long as standard PPE and dust control measures remain in place. Compared to more volatile or shock-sensitive oxidants, it offers peace of mind in daily routines.

    How It Differs from Other Products—Facts, Not Claims

    Oxidizing agents form a diverse crowd, from common bleach (sodium hypochlorite) and potassium permanganate to hydrogen peroxide, performic acid, and beyond. Each has strengths, but real distinctions emerge during hands-on use. mCPBA stands out for moderate oxidative strength—more robust than hydrogen peroxide, less aggressive and hazardous than peracetic acid. Many chemists have stories of mishaps involving more unmanageable reagents: uncontrolled reactions, safety alarms, disposal headaches. In my own practice, mCPBA rates far fewer calls to the environmental health and safety (EHS) office, especially when compared to chromic acid or nitric acid oxidations, which not only raise toxicity concerns but generate heavy-metal waste needing costly treatment.

    Hydrogen peroxide offers a green profile and lower cost, but outside select reactions, its lack of reactivity can drive frustration, requiring catalysts, longer reaction times, or elevated temperatures that put sensitive molecules at risk. On the other hand, peracetic acid packs a punch, but the cost is nervousness: its volatility and decomposition risks push caution to the limit. I’ve witnessed colleagues discard entire reaction batches after out-of-spec peracetic acid veered into explosive territory. mCPBA offers a smoother working experience: high enough oxidation potential for challenging tasks, yet straightforward warehousing and simple quenching protocols. Chlorinated byproducts—common with some other oxidants—are less of an issue, cutting down cleanup costs and environmental impact.

    Waste handling also draws a line in the sand. Anyone running a green chemistry program knows how quickly regulations and disposal costs rise with heavy metals or hazardous solvents. Byproducts from mCPBA degrade with routine neutralization, leaving less problematic residues for waste teams. In supervising undergraduate labs, I found this especially helpful: less hazardous waste means smoother compliance and fewer after-hours incident reports. The environmental data—while not perfect—speaks to a lessened footprint compared to many legacy oxidants still in use in older protocols.

    Safety, Handling, and Real-World Challenges

    Safety paints another clear distinction. Chemical oxidants have a reputation for unpredictability, yet mCPBA, in my years of hands-on use, consistently delivers safety with competence. With stable storage guidelines—low humidity, stable temperatures, sealed bottles—accidents stay rare. The biggest practical concern comes from dust. Proper PPE—nitrile gloves, lab protective glasses, and, where necessary, masks—cuts the risk. On plant visits, operators routinely point to mCPBA as “one of the easy ones” among the required oxidants, citing few recorded incidents and manageable cleanup protocols. Their confidence isn’t misplaced. Peroxides demand respect, but mCPBA rewards it with predictable behavior during weighing, mixing, and reactions.

    Still, underestimating any oxidizer can lead to trouble. Cases of bulk powder mishandling or accidental contact with organic solvents stress the need for good SOPs and regular safety training. In teaching labs, instructors hammer home that it only takes one poorly managed jar of reactive solid to cause headaches or heart-stopping close calls. Proper segregation, clear labeling, and periodic shelf audits prove crucial. If you’ve ever seen the aftermath of a mishandled oxidant—yellowed benches, melted plastic, and panicked calls—you appreciate the cool heads mCPBA allows. EMS rarely gets called for this one, and that builds trust over the years among experienced researchers and production workers alike.

    Solving Problems with Real Chemistry, Not Empty Promises

    In discussing solutions to ongoing chemical challenges, it’s easy to overlook how a well-chosen reagent like mCPBA can streamline research and production in ways far more complex tools simply can’t. Tackling problematic transformations—especially for medicinal chemists facing challenging functional groups or intricate molecular architectures—calls for a tool that lets the rest of the workflow fall in line. mCPBA lets late-stage oxidations run with fewer hiccups, lowering the odds that earlier investments in synthesis will be lost in a failed final step. Reducing purification stages cuts solvent use, operational time, and turnaround for new synthetic targets, a blessing for those of us on the clock against tight project timelines.

    Scale-up always brings worries: a reaction’s success on milligram scale rarely predicts success in kilo batches. mCPBA’s track record makes pilot plant teams relax, knowing the same selectivity and yields seen in glassware can be preserved in reactors. Its manageable exotherm and absence of shock sensitivity prove lifesavers; keeping production staff out of harm’s way remains a priority. In roundtable discussions, chemists almost universally place a premium on avoiding costly surprises during tech transfer and regulatory review. So, a proven, consistent oxidizing agent with decades of documented success wins points again and again over “greener” but less predictable alternatives, especially in blockbuster drug and specialty chemical synthesis.

    Approaching waste, many institutions are shifting toward smarter management and greener upstream choices. Here, too, mCPBA holds attention for its relatively benign waste profiles and straightforward aqueous quenching. The environmental health teams I’ve consulted with appreciate the simplicity of protocols: neutralize residual oxidant, extract byproducts, and move on. Regulations keep shifting toward lower impact, sustainable practices, and mCPBA’s real-world profile offers smoother compliance compared to more problematic reagents still entrenched by tradition.

    User Experience: Field Notes from the Bench and Beyond

    No introduction to a chemical’s capabilities feels complete without acknowledging daily user experience. The clearest feedback comes not from marketing but from benches stacked with decades of successful—and failed—syntheses. For many, mCPBA isn’t just another line in the reagent catalog; it’s a legacy tool that’s helped generations of chemists win hard fights in organic synthesis. The stories I hear from colleagues—whether in university teaching labs or in high-throughput process R&D—share a common theme: trust. Being able to depend on a reagent that does what’s expected, batch after batch, reshapes how work gets done. Even students new to chemistry catch on quickly, gaining confidence as results line up with textbook predictions.

    The value of consistent, reliable data can’t be overstated. Modern analytical tools pick apart side products and trace contaminants, but needing them less often saves both time and sanity. With mCPBA, researchers gain time to focus on next steps, not damage control. Practical details—such as odor, dust, spill risk, and handling protocols—mean more in the field than in paper spec sheets. Having supervised both teaching and production environments, I see firsthand how mCPBA fits into the daily rhythm, offering a combination of power and manageability that’s rare among reactive chemicals.

    Weighing the Future: Lessons for Sustainable Chemistry

    Sustainable chemistry doesn’t progress through wishful thinking. It moves forward through careful reagent choice, efficient reactions, and safer working conditions. 3-Chloroperoxybenzoic Acid—despite its age—holds up under these requirements. Its byproducts demand less effort for safe disposal and don’t saddle operators with persistent toxic or environmentally damaging residues. Its predictability helps new and veteran chemists keep timelines tight and budgets in check. For companies under tight regulatory pressure, having a reagent profile that rings fewer alarm bells locally and internationally can make a crucial difference.

    Safety will always be top of mind. With growing attention to occupational exposure limits, hazard communication, and emergency preparedness, labs and plants want reagents that perform without raising the risk floor. Having one less variable to manage frees up time and attention for critical innovation. Process engineers tell me that, in risk assessments, mCPBA sits well above alternatives with trickier thermal properties or breakdown products. This track record keeps it in toolkits around the world, at home in both legacy and cutting-edge manufacturing environments.

    Cost also makes waves in company boardrooms. Supplies of high-purity mCPBA keep production predictable, making it possible to plan multi-month synthesis campaigns with confidence. Predictable pricing and widely available supply mean lower procurement risk and more stable production schedules. This benefit trickles through value chains, as lower downtime means more product for less cost, whether in pharmaceuticals or specialty fine chemicals.

    Room for Improvement and Responsible Use

    No product is without its downsides. mCPBA carries its own risks—dust inhalation, corrosivity, limited compatibility with certain materials. Working alongside health and safety professionals, I’ve watched labs tighten up personal protective equipment rules and adapt fume hoods specifically for peracid management. Industry-wide, companies focus on finding bulk packaging methods that limit exposure while keeping the product dry and stable. There’s also continual progress in automating handling, weighing, and dosing, which further removes operators from front-line risk. As more chemists turn to flow chemistry and microreactor technology, mCPBA can be dosed more precisely, with less human intervention and exposure, building a safer, cleaner working future.

    The global chemical community is watching these shifts closely. Conversations about new oxidizing agents with even lower environmental footprints or reduced toxicological impacts are lively. Still, new options must perform in the complexity of real labs and plants—a bar that mCPBA cleared decades ago, and continues to meet today. I see this across industries: new green oxidants garner excitement, but scale-up failures or poor selectivity often send companies back to the drawing board. 3-Chloroperoxybenzoic Acid endures not from lack of alternatives, but through a proven balance of efficiency, availability, and manageable hazard profile.

    The Verdict—Experience Holds Weight

    Success in chemistry rests on well-worn tools as much as on innovation. mCPBA has become one of these—part of the backbone that allows new discoveries, streamlined production, and practical learning in labs scattered across continents. Its role in organic synthesis, pharmaceuticals, and specialized material production is built on both hard data and shared experience. As the global push toward greener, safer, and more efficient chemical manufacturing accelerates, this enduring reagent remains a benchmark—measured not just by specs, but by real-world outcomes and the trust of generations of chemists. Selecting 3-Chloroperoxybenzoic Acid is seldom exciting, but often the smartest move for those looking to advance research or scale production without surprise setbacks. Over years of hands-on and managerial experience, that quiet dependability is worth its weight in gold.